ClearanceBrief
510(k) K960230 ยท FDI Snare, Flexible

SNARE

ApplicantLighthouse Medical, Inc., Waltham MA, US
DecisionSubstantially Equivalent, Jul 31, 1996
ReceivedJan 17, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K960230

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.